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EC number: 201-796-4 | CAS number: 88-09-5
- Life Cycle description
- Uses advised against
- Endpoint summary
- Appearance / physical state / colour
- Melting point / freezing point
- Boiling point
- Density
- Particle size distribution (Granulometry)
- Vapour pressure
- Partition coefficient
- Water solubility
- Solubility in organic solvents / fat solubility
- Surface tension
- Flash point
- Auto flammability
- Flammability
- Explosiveness
- Oxidising properties
- Oxidation reduction potential
- Stability in organic solvents and identity of relevant degradation products
- Storage stability and reactivity towards container material
- Stability: thermal, sunlight, metals
- pH
- Dissociation constant
- Viscosity
- Additional physico-chemical information
- Additional physico-chemical properties of nanomaterials
- Nanomaterial agglomeration / aggregation
- Nanomaterial crystalline phase
- Nanomaterial crystallite and grain size
- Nanomaterial aspect ratio / shape
- Nanomaterial specific surface area
- Nanomaterial Zeta potential
- Nanomaterial surface chemistry
- Nanomaterial dustiness
- Nanomaterial porosity
- Nanomaterial pour density
- Nanomaterial photocatalytic activity
- Nanomaterial radical formation potential
- Nanomaterial catalytic activity
- Endpoint summary
- Stability
- Biodegradation
- Bioaccumulation
- Transport and distribution
- Environmental data
- Additional information on environmental fate and behaviour
- Ecotoxicological Summary
- Aquatic toxicity
- Endpoint summary
- Short-term toxicity to fish
- Long-term toxicity to fish
- Short-term toxicity to aquatic invertebrates
- Long-term toxicity to aquatic invertebrates
- Toxicity to aquatic algae and cyanobacteria
- Toxicity to aquatic plants other than algae
- Toxicity to microorganisms
- Endocrine disrupter testing in aquatic vertebrates – in vivo
- Toxicity to other aquatic organisms
- Sediment toxicity
- Terrestrial toxicity
- Biological effects monitoring
- Biotransformation and kinetics
- Additional ecotoxological information
- Toxicological Summary
- Toxicokinetics, metabolism and distribution
- Acute Toxicity
- Irritation / corrosion
- Sensitisation
- Repeated dose toxicity
- Genetic toxicity
- Carcinogenicity
- Toxicity to reproduction
- Specific investigations
- Exposure related observations in humans
- Toxic effects on livestock and pets
- Additional toxicological data
Endpoint summary
Administrative data
Description of key information
2-Ethylbutyric acid was shown to have a No Observed Adverse Effect Level (NOAEL) of 300 mg/kg bw/day in rats as part of a 14-day repeated dose toxicity (oral) experiment. A combined repeated dose and reproductive / developmental toxicity experiment was performed for 2-ethylbutyric acid over a 42-day period, in which there was a reported decrease in white blood cells at 50 mg/kg bw/day and in platelet count at 250 mg/kg bw/day in male rats. Following necropsy, kidney weight was reported to be significantly higher at 250 mg/kg bw/day in male and female rats. The NOAEL was subsequently considered to be 10 mg/kg bw/day in males and 50 mg/kg bw/day in females. The results of this experiment have been selected for the purpose of the endpoint conclusion given that they are more conservative and they have been obtained in a key study (Klimisch score = 2).
Key value for chemical safety assessment
Repeated dose toxicity: via oral route - systemic effects
Link to relevant study records
- Endpoint:
- short-term repeated dose toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- supporting study
- Study period:
- 1978
- Reliability:
- 4 (not assignable)
- Rationale for reliability incl. deficiencies:
- other: Insufficient information for an assessment of reliability.
- Principles of method if other than guideline:
- Not available
- GLP compliance:
- not specified
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male
- Route of administration:
- oral: feed
- Duration of treatment / exposure:
- 14 days
- Control animals:
- yes, concurrent no treatment
- Key result
- Dose descriptor:
- NOAEL
- Effect level:
- 300 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male
- Conclusions:
- In a 14-day repeated dose experiment for oral toxicity, 2-ethylbutyric acid was determined to have a No Observed Adverse Effect Level (NOAEL) of 300 mg/kg bw/day. The Lowest Observed Adverse Effect Level (LOAEL) could not be calculated.
- Endpoint:
- short-term repeated dose toxicity: oral
- Type of information:
- experimental study
- Adequacy of study:
- key study
- Study period:
- 2001
- Reliability:
- 2 (reliable with restrictions)
- Rationale for reliability incl. deficiencies:
- guideline study with acceptable restrictions
- Reason / purpose for cross-reference:
- reference to same study
- Qualifier:
- according to guideline
- Guideline:
- OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test)
- GLP compliance:
- yes
- Species:
- rat
- Strain:
- Sprague-Dawley
- Sex:
- male/female
- Route of administration:
- oral: gavage
- Duration of treatment / exposure:
- Males were dosed for a 42-day period that began 14 days before mating. Females were dosed 14 days prior to mating up until day 4 of lactation (i.e. during mating and pregnancy).
- Frequency of treatment:
- Once per day
- Dose / conc.:
- 0 mg/kg bw/day (nominal)
- Remarks:
- Control
- Dose / conc.:
- 10 mg/kg bw/day (nominal)
- Dose / conc.:
- 50 mg/kg bw/day (nominal)
- Dose / conc.:
- 250 mg/kg bw/day (nominal)
- No. of animals per sex per dose:
- 13 males and 13 females per dose
- Control animals:
- yes, concurrent vehicle
- Observations and examinations performed and frequency:
- Body weight (gain), food consumption, haematological findings, and biochemical findings of males / females. Estrous cycle in females.
- Sacrifice and pathology:
- Macroscopic findings, histopathological findings, and organ weight in males / females.
- Clinical signs:
- effects observed, treatment-related
- Description (incidence and severity):
- Transient salivation was observed in one male and one female at 250 mg/kg bw/day.
- Mortality:
- no mortality observed
- Description (incidence):
- No deaths related to the substance.
- Body weight and weight changes:
- no effects observed
- Food consumption and compound intake (if feeding study):
- no effects observed
- Haematological findings:
- effects observed, treatment-related
- Description (incidence and severity):
- No effect in females. Males exhibited decreased white blood cell count at ≥50 mg/kg bw/day and decreased platelet count at 250 mg/kg bw/day.
- Clinical biochemistry findings:
- effects observed, treatment-related
- Description (incidence and severity):
- No affect on blood chemistry and biochemical findings in males, although females exhibted significantly different y-GTP, total bilirubin, and Ca at 50 mg/kg bw/day and y-GTP at 250 mg/kg bw/day.
- Organ weight findings including organ / body weight ratios:
- effects observed, treatment-related
- Description (incidence and severity):
- At 250 mg/kg bw/day, male rats experienced increased relative kidney weight and females experienced increased absolute and relative kidney weight.
- Gross pathological findings:
- no effects observed
- Description (incidence and severity):
- No significant effects were found following necropsy.
- Histopathological findings: non-neoplastic:
- no effects observed
- Description (incidence and severity):
- No significant toxicological effects were found following necropsy.
- Histopathological findings: neoplastic:
- no effects observed
- Description (incidence and severity):
- No significant toxicological effects were found following necropsy.
- Other effects:
- effects observed, treatment-related
- Description (incidence and severity):
- No adverse effects were observed on reproductive parameters, such as estrous cycle, copulation index, fertility index, precoital interval, gestation length, numbers of corpora lutea and implantations, gestation index, implantation index and delivery index. Birth index and live birth index was lower for the 250 mg/kg bw/day treatment group.
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- Repeated dose toxicity
- Effect level:
- 10 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- male
- Remarks on result:
- other: Additional information not available
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- Repeated dose toxicity
- Effect level:
- 50 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- female
- Remarks on result:
- other: Additional information not available
- Key result
- Dose descriptor:
- NOAEL
- Remarks:
- Reproductive toxicity
- Effect level:
- 250 mg/kg bw/day (nominal)
- Based on:
- test mat.
- Sex:
- female
- Remarks on result:
- other: Additional information not available
- Key result
- Critical effects observed:
- yes
- Lowest effective dose / conc.:
- 50 mg/kg bw/day (nominal)
- System:
- haematopoietic
- Organ:
- blood
- leucocyte development
- Treatment related:
- yes
- Dose response relationship:
- not specified
- Relevant for humans:
- not specified
- Key result
- Critical effects observed:
- yes
- Lowest effective dose / conc.:
- 250 mg/kg bw/day (nominal)
- System:
- haematopoietic
- Organ:
- blood
- platelet formation
- Treatment related:
- yes
- Dose response relationship:
- not specified
- Relevant for humans:
- not specified
- Key result
- Critical effects observed:
- yes
- Lowest effective dose / conc.:
- 250 mg/kg bw/day (nominal)
- System:
- urinary
- Organ:
- kidney
- Treatment related:
- yes
- Dose response relationship:
- not specified
- Relevant for humans:
- not specified
- Conclusions:
- 2-Ethylbutyric acid was determined to have a NOAEL for reproductive toxicity and developmental toxicity of 250 and 50 mg/kg bw/day, respectively. A NOAEL for repeated dose toxicity was concluded to be 10 mg/kg bw/day in males and 50 mg/kg bw/day in females. These results were the outcome of a combined repeated dose (42-day) and developmental / reproductive toxicity test in male and female rats.
- Executive summary:
A combined experiment was undertaken to determine the repeated dose toxicity and developmental / reproductive toxicity of 2-ethylbutyric acid in male and female rats. Animals were administered the substance in a corn oil vehicle via oral gavage once per day for a total of 42 days at doses of 0 (control), 10, 50, or 250 mg/kg bw/day. The experiment was performed in line with Good Laboratory Practise (GLP) and OECD Guideline 422 (Combined Repeated Dose Toxicity Study with the Reproduction / Developmental Toxicity Screening Test).
No mortality was recorded over the duration of the test that was related to 2-ethylbutyric acid. Transient salivation in males / females (250 mg/kg bw/day); decreased white blood cell count (50 mg/kg bw/day) and platelet count (250 mg/kg bw/day) in males; increased kidney weight in males / females (250 mg/kg bw/day); decreased live pups on day 0 and 4 of lactation (250 mg/kg bw/day); and decreased birth index and live birth index (250 mg/kg bw/day) was recorded. No significantly negative effects were observed in males and females relating to body weight gain; food intake; blood chemistry; necropsy; histopathology; and reproductive parameters (e.g. estrous cycle, copulation index). There were no treatment-related changes in body weight, external appearance, and necropsy findings in rat pups.
2-Ethylbutyric acid was determined to have a NOAEL of 250 and 50 mg/kg bw/day for reproductive toxicity and developmental toxicity, respectively. A NOAEL for repeated dose toxicity was concluded to be 10 mg/kg bw/day in males and 50 mg/kg bw/day in females.
Referenceopen allclose all
F1 Generation
No treatment-related change in external appearance. Number of live pups at 250 mg/kg bw/day was lower than control (0 mg/kg bw/day) and other treatment groups. No treatment-related change in body weight.
Endpoint conclusion
- Endpoint conclusion:
- adverse effect observed
- Dose descriptor:
- NOAEL
- 10 mg/kg bw/day
- Study duration:
- subchronic
- Species:
- rat
Additional information
Justification for classification or non-classification
Information on Registered Substances comes from registration dossiers which have been assigned a registration number. The assignment of a registration number does however not guarantee that the information in the dossier is correct or that the dossier is compliant with Regulation (EC) No 1907/2006 (the REACH Regulation). This information has not been reviewed or verified by the Agency or any other authority. The content is subject to change without prior notice.
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